Device recall
Z-0923-2026: Brand name: AGFA Digital Radiography X- Ray system DR 800 with MUSICA Dynamic…
FDA device recall · Class II · AGFA Healthcare Corp.
Key facts
| Recall number (Z-number) | Z-0923-2026 |
|---|---|
| Recall event | 98101 |
| Product | Brand name: AGFA Digital Radiography X- Ray system DR 800 with MUSICA Dynamic Common Name: DR 800 |
| Product code | IZF |
| Recalling firm | AGFA Healthcare Corp. |
| Recall class | Class II |
| Status | Open, Classified |
| 510(k) numbers | K183275 |
| FEI number | 3001236302 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 1–9 Recalled products with this product code
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA device recalls (products)
Each recalled device product receives a Z-number. Recall details such as root cause, distribution and firm actions are available in Orca1.
Source: U.S. Food and Drug Administration (FDA), Medical Device Recalls database